≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Store at -20°C Ships Ice chest + Ice pads Check lot-specific COA for exact specifications.
SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
BLT-1 (Block lipid transport-1) has been used as an inhibitor of the SR-BI (scavenger receptor, class B, type I) mediated lipid transfer to determine if miR-223-3p export from polymorphonuclear neutrophils (PMNs) to high-density lipoproteins (HDLs) is dependent on SR-BI-mediated lipid flux. It has also been used as a SR-BI inhibitor to study the effect of HDL on osteocalcin (OCN) expression in monocyte cell lines through SR-B1.
BLT-1 may be used to study cell signaling pathways that have role in cholesterol influx and efflux.
| Sonrisas canónicas | CCCCCCC1CCCC1=NNC(=S)N |
|---|---|
| IUPAC Name | [(E)-(2-hexylcyclopentylidene)amino]thiourea |
| InChIKey | OWGUSBISUVLUJF-SDNWHVSQSA-N |
| INCHI | 1S/C12H23N3S/c1-2-3-4-5-7-10-8-6-9-11(10)14-15-12(13)16/h10H,2-9H2,1H3,(H3,13,15,16)/b14-11+ |
| Isómeros SMILES | CCCCCCC\1CCC/C1=N\NC(=S)N |
| WGK Alemania | 3 |
| Peso molecular | 241.4 |
| Reaxy-Rn | 11250336 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=11250336&ln= |
Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS →Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA →Full quality attributes and acceptance criteria for this grade.
View spec sheet →Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Organic nitrogen compounds |
| Clase | Organonitrogen compounds |
| Subclass | Hydrazines and derivatives |
| Intermediate Tree Nodes | Thiosemicarbazides |
| Direct Parent | Thiosemicarbazones |
| Alternative Parents | Organosulfur compounds Hydrocarbon derivatives |
| Molecular Framework | Aliphatic homomonocyclic compounds |
| Substituents | Thiosemicarbazone - Hydrocarbon derivative - Organosulfur compound - Aliphatic homomonocyclic compound |
| Descripción | This compound belongs to the class of organic compounds known as thiosemicarbazones. These are compounds containing the thiosemicarbazone functional group obtained by replacing the carbonyl group by a thiocarbonyl group. |
| External Descriptors | Not available |
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Fecha | Articulo |
|---|---|---|---|
 A2420068 | Certificate of Analysis | Dec 19, 2023 | B412587 |
| A2420069 | Certificate of Analysis | Dec 19, 2023 | B412587 |
| A2420070 | Certificate of Analysis | Dec 19, 2023 | B412587 |
| A2420071 | Certificate of Analysis | Dec 19, 2023 | B412587 |
| A2420072 | Certificate of Analysis | Dec 19, 2023 | B412587 |
| Solubilidad | DMSO: ≥13 mg/mL |
|---|---|
| Peso molecular | 241.400 g/mol |
| XLogP3 | 3.300 |
| Hydrogen Bond Donor Count | 2 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 6 |
| Exact Mass | 241.161 Da |
| Monoisotopic Mass | 241.161 Da |
| Topological Polar Surface Area | 82.500 Ų |
| Heavy Atom Count | 16 |
| Formal Charge | 0 |
| Complexity | 251.000 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 1 |
| Defined Bond Stereocenter Count | 1 |
| Undefined Bond Stereocenter Count | 0 |
| The total count of all stereochemical bonds | 1 |
| Covalently-Bonded Unit Count | 1 |
